构建 C(sp3)-C(sp3)键的还原亲电交叉偶联反应

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC Synlett Pub Date : 2024-07-25 DOI:10.1055/a-2373-0471
Pengfei Li, Youai Qiu
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引用次数: 0

摘要

C(sp3)-C(sp3)键是有机化合物中最常见的主题之一,在有机合成中具有重要意义。利用两个烷基亲电体进行交叉耦合是建立 C(sp3)-C(sp3)键的重要策略。如今,合成电化学正处于快速发展阶段,因为它不仅具有减少大量传统化学还原剂的绿色经济特性,还能在温和条件下生成高活性自由基中间体,从而开辟新的反应途径,为构建 C(sp3)-C(sp3)键提供新的机会。本文旨在全面阐述传统亲电试剂在构建 C(sp3)-C(sp3)键方面的历史发展,同时深入探讨电化学亲电交叉偶联在这一领域的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Reductive Electrophilic Cross-Coupling for Constructing C(sp3)–C(sp3) Bonds
C(sp3)-C(sp3) bond is one of the most prevalent motifs in organic compounds and holds significant importance in organic synthesis. The utilization of two alkyl electrophiles for cross-coupling stands as a vital strategy in building C(sp3)–C(sp3) bonds. Nowadays, synthetic electrochemistry is undergoing rapid development owing to its exceptional attributes not only in terms of green and economic properties by reducing the large amount of traditional chemical reductants, but also by its capacity to generate highly reactive radical intermediates under mild conditions, thereby opening up new reaction pathways and presenting novel opportunities to constructing C(sp3)-C(sp3) bonds. This article aims to comprehensively delineate the historical development of traditional electrophilic reagents in constructing C(sp3)-C(sp3) bonds, while also delving into the advantages of electrochemical electrophilic cross-coupling in this domain.
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来源期刊
Synlett
Synlett 化学-有机化学
CiteScore
3.40
自引率
5.00%
发文量
369
审稿时长
1 months
期刊介绍: SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.
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